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The treatment of chronic hepatitis C in HIV-infected patients: a meta-analysis
1Division of Infectious Diseases, VA Greater Los Angeles Healthcare System, Los Angeles, CA, USA.
Insights
Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) coinfection accelerates disease. Peginterferon plus ribavirin significantly improves sustained virological response in coinfected patients without increasing adverse events.
Area of Science:
- Hepatology
- Virology
- Infectious Diseases
Background:
- Hepatitis C virus (HCV) coinfection with human immunodeficiency virus (HIV) accelerates disease progression.
- The increasing lifespan of coinfected patients necessitates understanding HCV management strategies.
- Previous studies suggest varying efficacy of interferon-based therapies for HCV in coinfected individuals.
Purpose of the Study:
- To evaluate the efficacy and safety of peginterferon plus ribavirin compared to interferon-based regimens for chronic HCV/HIV coinfection.
- To analyze sustained virological response (SVR) rates across different HCV genotypes.
- To assess safety concerns, including severe adverse effects and treatment withdrawal rates.
Main Methods:
- Systematic review and meta-analysis of prospective randomized controlled trials (RCTs).
- Searched MEDLINE and Cochrane databases (1966-2005) and national meeting abstracts (2001-2005).
- Included trials comparing peginterferon plus ribavirin against peginterferon or interferon plus ribavirin.
Main Results:
- Peginterferon plus ribavirin demonstrated significantly higher SVR rates compared to interferon plus ribavirin (OR 3.00).
- This benefit was observed across HCV genotypes 1/4 (OR 4.40) and 2/3 (OR 2.56).
- Peginterferon plus ribavirin also showed higher SVR than peginterferon monotherapy (OR 2.60), with similar rates of severe adverse effects and withdrawal.
Conclusions:
- Peginterferon plus ribavirin is a more effective treatment for achieving SVR in patients with chronic HCV/HIV coinfection.
- This combination therapy offers improved outcomes without a significant increase in serious adverse events or treatment discontinuation.
- These findings support the use of peginterferon plus ribavirin for managing HCV in coinfected populations.
Objective:
Hepatitis C virus (HCV) disease progression appears to be accelerated in patients coinfected with HIV. The impact of HCV on coinfected patients is being realized as patients are now living longer. The objective of our study was to further elucidate incremental improvement and safety concerns with combinations of pegylated interferon (peginterferon), interferon and ribavirin based on data obtained from prospective randomized controlled trials.
Methods:
A search of MEDLINE and the Cochrane database for material published between 1966 and 29 August 2005 and a hand search of abstracts from national meetings held between 2001 and August 2005 were performed. Trials comparing the use of peginterferon plus ribavirin vs peginterferon or interferon plus ribavirin were assessed.
Results:
In six randomized controlled trials, 1756 patients were randomized. Sustained virological response was greater for patients treated with peginterferon plus ribavirin compared with patients treated with interferon plus ribavirin [odds ratio (OR) 3.00; 95% confidence interval (CI) 2.27-3.96]. This increased sustained virological response with peginterferon and ribavirin was found for patients with HCV genotype 1 or 4 (OR 4.40; 95% CI 2.75-7.03) and genotype 2 or 3 (OR 2.56; 95% CI 1.71-3.85). Sustained virological responses were also higher with peginterferon and ribavirin as compared with peginterferon monotherapy (OR 2.60; 95% CI 1.84-3.67). Severe adverse effects (OR 1.09; 95% CI 0.74-1.4) and withdrawal rates (OR 0.97; 95% CI 0.75-1.25) were similar between patients treated with peginterferon plus ribavirin and patients treated with interferon plus ribavirin.
Conclusions:
Patients with chronic HCV/HIV coinfection have a greater likelihood of achieving a sustained virological response with peginterferon plus ribavirin. The likelihoods of serious adverse effects and study withdrawal were similar.
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